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Schwartz–Jampel syndrome with gastroduodenal bleeding

Schwartz–Jampel syndrome is a rare autosomal recessive disorder with joint contractures, generalized myotonia, skeletal anomalies, and facial dysmorphism. The patients with Schwartz–Jampel syndrome have muscle stiffness and electromyography reveals complex, repetitive discharges as myotonic discharg...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Pediatr Neurosci
Prif Awduron: Polat, İpek, Karaoğlu, Pakize, Yiş, Uluç, Kurul, Semra Hız
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Medknow Publications & Media Pvt Ltd 2016
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5108135/
https://ncbi.nlm.nih.gov/pubmed/27857801
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.193351
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